鈻狿laying an important role in handling of all regulatory audits like USFDA,EUGMP,TGA,INVIMA,ANVISA,TFDA(Taiwan),TFDA(Tanzania),GCC.
鈻狹arket complaint response review and investigations,
鈻� Review of Batch records and releases of batches as per cGMP compliance,
鈻� Handling of deviation, change controls and CAPA,
鈻� Handling of out of specification results and out of trend results,
鈻� Ensure compliances of Quality systems during batch manufacturing, packing and other activities,
鈻� Master document review.
鈻� Coordination with internal and external customers for Quality related issues: technical agreements and batch related query and responses,
鈻� Coordination with all other dep...
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